Xu Wei-Teng, Lu Xin-Yu, Wang Yue, Li Ming-Han, Hu Ke, Shen Zi-Jie, Sun Xiao-Qin, Zhang Yan-Mei
Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing 210014, China.
Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Nanjing 210014, China.
J Fungi (Basel). 2024 Apr 26;10(5):315. doi: 10.3390/jof10050315.
The greater yam (), a widely cultivated and nutritious food crop, suffers from widespread yield reduction due to anthracnose caused by . Latent infection often occurs before anthracnose phenotypes can be detected, making early prevention difficult and causing significant harm to agricultural production. Through comparative genomic analysis of 60 genomes of 38 species from the genus, this study identified 17 orthologous gene groups (orthogroups) that were shared by all investigated strains but absent from all other species. Four of the 17 -specific orthogroups were used as molecular markers for PCR primer designation and detection. All of them can specifically detect out of microbes within and beyond the genus with different sensitivities. To establish a rapid, portable, and operable anthracnose diagnostic method suitable for field use, specific recombinase polymerase amplification (RPA) primer probe combinations were designed, and a lateral flow (LF)-RPA detection kit for was developed, with the sensitivity reaching the picogram (pg) level. In conclusion, this study identified -specific molecular markers and developed an efficient method for detection, which can be applied to the prevention and control of yam anthracnose as well as anthracnose caused by in other crops. The strategy adopted by this study also serves as a reference for the identification of molecular markers and diagnosis of other plant pathogens.
大薯是一种广泛种植且营养丰富的粮食作物,因炭疽菌引起的炭疽病而普遍减产。在炭疽病表型能够被检测到之前,潜伏感染常常已经发生,这使得早期预防变得困难,并对农业生产造成重大损害。通过对薯蓣属38个物种的60个基因组进行比较基因组分析,本研究鉴定出17个直系同源基因组(直系同源群),这些直系同源基因组为所有被研究的炭疽菌菌株所共有,但在所有其他薯蓣属物种中不存在。这17个炭疽菌特异性直系同源基因组中的4个被用作PCR引物设计和炭疽菌检测的分子标记。它们都能以不同的灵敏度特异性检测出炭疽菌属内外的微生物。为建立一种适用于田间使用的快速、便携且可操作的炭疽病诊断方法,设计了特异性重组酶聚合酶扩增(RPA)引物探针组合,并开发了一种用于炭疽菌检测的侧向流动(LF)-RPA检测试剂盒,其灵敏度达到皮克(pg)水平。总之,本研究鉴定出了炭疽菌特异性分子标记,并开发了一种高效的炭疽菌检测方法,该方法可应用于大薯炭疽病以及其他作物中炭疽菌引起的炭疽病的防控。本研究采用的策略也为其他植物病原体的分子标记鉴定和诊断提供了参考。